Feedback on Perioperative Temperature Management and Patient Outcomes: Three-arm Trial to Compare Feedback
Sponsor
Ottawa Hospital Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT02414191
Collaborator
(none)
45
1
3
38.1
1.2
Study Details
Study Description
Brief Summary
The investigators aim to assess the impact of benchmarked and ranked feedback on anesthesiologists' perioperative temperature management and subsequent patient outcomes.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Study Type:
Interventional
Actual Enrollment
:
45 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Health Services Research
Official Title:
Effect of Audit and Feedback on Physicians' Perioperative Temperature Management and Patient Outcomes: A Three-arm Cluster Randomized Controlled Trial to Compare Benchmarked and Ranked Feedback
Actual Study Start Date
:
Feb 1, 2015
Actual Primary Completion Date
:
Apr 6, 2018
Actual Study Completion Date
:
Apr 6, 2018
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| No Intervention: Control Participants in this study arm will receive no form of feedback. |
|
| Other: Benchmarked Feedback Participants in this study arm will receive benchmarked feedback regarding their perioperative temperature management. |
Behavioral: Benchmarked Feedback
Participants receive data, during the 6 month intervention phase, regarding their monthly temperature management performance in the form of benchmarked feedback, which is the measure of their performance in comparison the standard set by the hospital.
|
| Other: Ranked Feedback Participants in this study arm will receive ranked feedback regarding their perioperative temperature management. |
Behavioral: Ranked Feedback
Participants receive data, during the 6 month intervention phase, regarding their monthly temperature management performance in the form of ranked feedback, which is the measure of their performance in comparison to their peers.
|
Outcome Measures
Primary Outcome Measures
- Patient peri-operative temperature [Within the 30 minutes immediately before or the 15 minutes immediately after anesthesia end time.]
Secondary Outcome Measures
- Intraoperative warming device usage perioperative [intraoperative]
- Patient post-operative surgical site infection (SSI) rate [Within 30 days of surgery]
Eligibility Criteria
Criteria
Ages Eligible for Study:
N/A
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- Staff Anesthesiologists at The Ottawa Hospital
Exclusion Criteria:
- none
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The Ottawa Hospital | Ottawa | Ontario | Canada | K1Y4E9 |
Sponsors and Collaborators
- Ottawa Hospital Research Institute
Investigators
- Principal Investigator: Sylvain Boet, MD, PhD, The Ottawa Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Ottawa Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT02414191
Other Study ID Numbers:
- 20140117-01H
First Posted:
Apr 10, 2015
Last Update Posted:
Mar 24, 2020
Last Verified:
Mar 1, 2020
Keywords provided by Ottawa Hospital Research Institute
Additional relevant MeSH terms: